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rs10789230

From SNPedia

Orientationplus
Stabilizedplus
Make rs10789230(G;G)
Make rs10789230(G;T)
Make rs10789230(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position67264945
is asnp
is mentioned by
dbSNPrs10789230
ebirs10789230
HLIrs10789230
Exacrs10789230
Varsomers10789230
Maprs10789230
PheGenIrs10789230
hapmaprs10789230
1000 genomesrs10789230
hgdprs10789230
ensemblrs10789230
gopubmedrs10789230
geneviewrs10789230
scholarrs10789230
googlers10789230
pharmgkbrs10789230
gwascentralrs10789230
openSNPrs10789230
23andMers10789230
23andMe allrs10789230
SNP Nexus

SNPshotrs10789230
SNPdbers10789230
MSV3drs10789230
GWAS Ctlgrs10789230
GMAF0.4086
Max Magnitude
GWAS
SNP rs10789230
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele
pValue 1.00E-008
OR 1.38
95% CI 1.23-1.53



GET Evidence
rs10789230
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.375
summary